Method for degrading lignin using visible-light response composite catalyst
A composite catalyst and visible light technology, which is applied in the field of effective utilization of lignin resources, can solve the problems of benzene ring damage and non-compliance, and achieve the effect of high benzene ring retention rate and simple and easy preparation method
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example 1
[0023] Mix 1g of refined lignin, 100mL of distilled water, 20mL of n-butanol, 0.020g of dimethyl ether quinoline squaraine (see attached figure 1 ), 0.0500g nano-TiO 2 (The particle size of the photocatalyst is 2nm~50nm) Avoid light and ultrasonically disperse for 20min, then irradiate with sunlight for 6h; after the reaction, let stand for 2h, then centrifuge at 8000rad / min at high speed, wash 3 times with distilled water, and the solid residue is degraded Lignin Ⅰ was then dissolved in alkali and acid-precipitated to obtain flocculent precipitates, and dried in vacuum at 80°C with a yield of 63.12%; DPPH free radical (1,1-diphenyl-2-trinitrobenzene Hydrazine, see attached Figure 4 ) Determination of antioxidant capacity: IC of lignin 50 (required concentration to remove 50% of DPPH free radicals) value is 0.199mg / mL; degraded lignin Ⅰ has higher antioxidant ability to DPPH free radicals than original lignin, and its IC 50 The value is 0.127mg / mL; compared with the common...
example 2
[0028] 1g refined lignin, 100mL distilled water, 20mL n-butanol, 0.02g ruthenium complex N3 dye [chemical name: CIS-dithiocyanatobis(N,N'-2,2'-bipyridine-4,4 '-diformic acid) ruthenium] (see attached figure 2 ), 0.0500g nano-TiO 2 (The particle size of the photocatalyst is 2nm~50nm) Avoid light and ultrasonically disperse for 20min, and then irradiate with sunlight for 6h; centrifuge after the reaction, discard the supernatant, and wash the remaining solid twice with an appropriate amount of distilled water; then dissolve in alkali, acid A flocculent precipitate was obtained, and after centrifugation, washing, and drying, the degraded lignin II was obtained with a yield of 45.82%; the degraded lignin II was subjected to DPPH free radical (1,1-diphenyl-2-trinitrophenylhydrazine, See attached Figure 4 ) Determination of antioxidant capacity: IC of lignin 50 (required concentration to remove 50% of DPPH free radicals) value is 0.199mg / mL; degraded lignin II has higher antioxid...
example 3
[0032] Mix 1g refined lignin, 100mL distilled water, 20mL n-butanol, 0.02g tetracarboxylic cobalt phthalocyanine (see attached image 3 ), 0.0500g nano-TiO 2 (The particle size of the photocatalyst is 2nm~50nm) Avoid light and ultrasonically disperse for 20min, and then irradiate with sunlight for 6h; centrifuge after the reaction, discard the supernatant, and wash the remaining solid twice with an appropriate amount of distilled water; then dissolve in alkali, acid A flocculent precipitate was obtained, and after centrifugation, washing, and drying, the lignin activation product III was obtained with a yield of 48.82%; the degraded lignin III was subjected to DPPH free radical (1,1-diphenyl-2-trinitrophenylhydrazine , see attached Figure 4 ) Determination of antioxidant capacity: IC of lignin 50 (required concentration to remove 50% of DPPH free radicals) value is 0.199mg / mL; degraded lignin Ⅲ has higher antioxidant ability to DPPH free radicals than original lignin, and i...
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